Major clinical and metabomic approaches to childhood obesity: a systematic review

Mauro Lopes Teixeira Filho, Anna Beatriz de Moraes Dourado
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Abstract

Introduction: In the context of childhood obesity, of children under 5 years of age in Brazil, 7% are overweight and 3% meet the criteria for obesity. Globally, according to a report from the World Health Organization (WHO), it is estimated that the total number of overweight and obese children in the world could reach 75 million by the year 2025. Objective: It was to carry out a systematic review to present the main approaches to clinical and metabolomics of childhood obesity. Methods: The PRISMA Platform systematic review rules were followed. The research was carried out from February to April 2024 in the Scopus, PubMed, Science Direct, Scielo and Google Scholar databases. The quality of the studies was based on the GRADE instrument and the risk of bias was analyzed according to the Cochrane instrument. Results and Conclusion: 110 articles were recruited for the initial evaluation. A total of 41 articles were evaluated and 19 were included in this systematic review. Considering the Cochrane tool for risk of bias, the overall assessment resulted in 28 studies with a high risk of bias and 28 studies that did not meet GRADE. Most studies showed homogeneity in their results, with X2=58.7%>50%. It was concluded that miRNAs are potential biomarkers for the development of pathologies, such as obesity. A heterogeneous group of these molecules was found to be associated with obesity in children. miR-15b-5p, miR-486-5p and hsa-miR-122-5p were considered good candidates for childhood obesity biomarkers. MiRNA-dependent mechanisms regulate up to 60% of all human genes. MiRNAs influence multiple pathways, including insulin signaling, immune-mediated inflammation, adipokine expression, adipogenesis, lipid metabolism, and regulation of food intake.
儿童肥胖症的主要临床和代谢组学方法:系统性综述
引言在儿童肥胖症方面,巴西 5 岁以下儿童中有 7%超重,3%达到肥胖标准。根据世界卫生组织(WHO)的一份报告,预计到 2025 年,全球超重和肥胖儿童总数将达到 7500 万。研究目的对儿童肥胖症的临床和代谢组学的主要方法进行系统综述。方法:遵循 PRISMA 平台系统综述规则。研究于 2024 年 2 月至 4 月在 Scopus、PubMed、Science Direct、Scielo 和 Google Scholar 数据库中进行。研究质量根据 GRADE 工具进行评估,偏倚风险根据 Cochrane 工具进行分析。结果与结论:初步评估共征集了 110 篇文章。共评估了 41 篇文章,其中 19 篇被纳入本系统综述。根据科克伦偏倚风险工具,总体评估结果为 28 项研究存在高偏倚风险,28 项研究不符合 GRADE 标准。大多数研究结果显示具有同质性,X2=58.7%>50%。结论是,miRNA 是肥胖等病理发展的潜在生物标志物。miR-15b-5p、miR-486-5p 和 hsa-miR-122-5p 被认为是儿童肥胖症生物标志物的理想候选者。依赖于 MiRNA 的机制可调控多达 60% 的人类基因。MiRNA 影响多种途径,包括胰岛素信号传导、免疫介导的炎症、脂肪因子表达、脂肪生成、脂质代谢和食物摄入调节。
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